ClinVar Miner

List of variants in gene SMARCAL1 reported as benign

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Gene type:
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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_014140.4(SMARCAL1):c.1851+293T>G rs284551 0.71834
NM_014140.4(SMARCAL1):c.2528+68T>C rs284523 0.36760
NM_014140.4(SMARCAL1):c.2528+131A>G rs205980 0.36542
NM_014140.4(SMARCAL1):c.2071-136T>C rs2129119 0.30191
NM_014140.4(SMARCAL1):c.1711-132G>A rs2738284 0.24411
NM_014140.4(SMARCAL1):c.2529-153T>G rs284524 0.24198
NM_014140.4(SMARCAL1):c.1335-91G>A rs2271334 0.21490
NM_014140.4(SMARCAL1):c.2070T>C (p.Thr690=) rs2066527 0.09632
NM_014140.4(SMARCAL1):c.1852-153A>G rs66931264 0.09543
NC_000002.12:g.216483194T>C rs17559422 0.09481
NM_014140.4(SMARCAL1):c.812-104T>C rs71577872 0.09447
NM_014140.4(SMARCAL1):c.1096+152A>G rs3816784 0.05438
NM_014140.4(SMARCAL1):c.812-156T>C rs2306638 0.05421
NM_014140.4(SMARCAL1):c.2528+198C>T rs78149672 0.05399
NM_014140.4(SMARCAL1):c.2428-95G>A rs58959714 0.05181
NM_014140.4(SMARCAL1):c.945C>G (p.Ser315Arg) rs2066522 0.04137
NM_014140.4(SMARCAL1):c.1335-23A>G rs2066521 0.03522
NM_014140.4(SMARCAL1):c.-58-254G>A rs58617956 0.03312
NM_014140.4(SMARCAL1):c.1129G>C (p.Glu377Gln) rs2066518 0.03294
NM_014140.4(SMARCAL1):c.1645-56T>C rs3816783 0.03291
NM_014140.4(SMARCAL1):c.2626-33C>T rs71579835 0.03207
NM_014140.4(SMARCAL1):c.-58-210G>A rs73072254 0.02897
NM_014140.4(SMARCAL1):c.2141+17T>C rs2066516 0.02324
NM_014140.4(SMARCAL1):c.862+183G>A rs73072255 0.02225
NM_014140.4(SMARCAL1):c.1711-106C>T rs79491615 0.02193
NM_014140.4(SMARCAL1):c.2626-191G>T rs79008053 0.02062
NM_014140.4(SMARCAL1):c.811+156T>C rs79736801 0.02034
NM_014140.4(SMARCAL1):c.812-89G>A rs75546339 0.01886
NM_014140.4(SMARCAL1):c.1711-283C>A rs16856180 0.01658
NM_014140.4(SMARCAL1):c.2428-350G>T rs75259438 0.01622
NM_014140.4(SMARCAL1):c.1711-119C>T rs284549 0.01596
NM_014140.4(SMARCAL1):c.1096+32A>C rs2066515 0.01592
NM_014140.4(SMARCAL1):c.2071-296G>A rs74434188 0.01531
NM_014140.4(SMARCAL1):c.2070+43A>T rs78230573 0.01522
NM_014140.4(SMARCAL1):c.127G>A (p.Ala43Thr) rs2066524 0.01441
NM_014140.4(SMARCAL1):c.423T>C (p.Tyr141=) rs35907255 0.00918
NM_014140.4(SMARCAL1):c.901C>G (p.Pro301Ala) rs146084305 0.00795
NM_014140.4(SMARCAL1):c.1243A>G (p.Ser415Gly) rs58848916 0.00728
NM_014140.4(SMARCAL1):c.341G>A (p.Arg114His) rs11555797 0.00693
NM_014140.4(SMARCAL1):c.1534G>A (p.Val512Met) rs35087810 0.00316
NM_014140.4(SMARCAL1):c.1212G>A (p.Ala404=) rs2066525 0.00241
NM_014140.4(SMARCAL1):c.603G>C (p.Gly201=) rs35048226 0.00234
NM_014140.4(SMARCAL1):c.1995C>T (p.Ala665=) rs151241914 0.00217
NM_014140.4(SMARCAL1):c.1271A>T (p.Asp424Val) rs2066520 0.00205
NM_014140.4(SMARCAL1):c.2528+15G>A rs200879397 0.00078
NM_014140.4(SMARCAL1):c.1850G>T (p.Arg617Leu) rs199805996 0.00068
NM_014140.4(SMARCAL1):c.124A>G (p.Ile42Val) rs199905841 0.00055
NM_014140.4(SMARCAL1):c.962G>A (p.Gly321Asp) rs148752234 0.00045
NM_014140.4(SMARCAL1):c.2244+19T>C rs752967601 0.00038
NM_014140.4(SMARCAL1):c.2226G>A (p.Thr742=) rs2271335 0.00031
NM_014140.4(SMARCAL1):c.270C>T (p.His90=) rs150591090 0.00029
NM_014140.4(SMARCAL1):c.1785C>T (p.Ile595=) rs145825654 0.00027
NM_014140.4(SMARCAL1):c.2649C>T (p.Tyr883=) rs182217350 0.00008
NM_014140.4(SMARCAL1):c.1056C>T (p.Asp352=) rs775747796 0.00003
NM_014140.4(SMARCAL1):c.72A>G (p.Arg24=) rs199805770 0.00001
NM_014140.4(SMARCAL1):c.1645-274C>T rs77349113
NM_014140.4(SMARCAL1):c.1711-111G>T rs284550
NM_014140.4(SMARCAL1):c.1852-205A>C rs2738286
NM_014140.4(SMARCAL1):c.1947C>T (p.Asp649=) rs2066526
NM_014140.4(SMARCAL1):c.2141+56dup rs34170201
NM_014140.4(SMARCAL1):c.2625+116dup rs5838586
NM_014140.4(SMARCAL1):c.340C>G (p.Arg114Gly) rs202031614
NM_014140.4(SMARCAL1):c.811+36_811+38del rs5838583
NM_014140.4(SMARCAL1):c.811+37_811+38del rs5838583
NM_014140.4(SMARCAL1):c.811+38del rs5838583
NM_014140.4(SMARCAL1):c.862+128del rs3214962
NM_014140.4(SMARCAL1):c.863-39C>G rs73988775
NM_014140.4(SMARCAL1):c.960C>T (p.Ala320=) rs2066513
NM_014140.4(SMARCAL1):c.961G>A (p.Gly321Ser) rs371378288

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